Salivary gland disorder

disease
On this page

Also known as disease of saliva-secreting glanddisease or disorder of saliva-secreting glanddisorder of saliva-secreting glandnon-neoplastic salivary gland diseasesaliva-secreting gland diseasesaliva-secreting gland disease or disordersalivary gland disease

Summary

Salivary gland disorder (MONDO:0001142) is a disease (an umbrella term covering 9 Mondo subtypes) with 3 GWAS associations across 23 studies and 14 clinical trials. Top therapeutic interventions include ciprofloxacin, prasterone, and honey. A subtype of mouth disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Umbrella term: 9 Mondo subtypes
  • GWAS associations: 3
  • Clinical trials: 14

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namesalivary gland disorder
Mondo IDMONDO:0001142
EFOEFO:0008581
MeSHD012466
DOIDDOID:10854
ICD-111432273670
NCITC26879
SNOMED CT10890000
UMLSC0149772
MedGen892384
Anatomy (UBERON)UBERON:0001044
Is cancer (heuristic)no

Also known as: disease of saliva-secreting gland · disease or disorder of saliva-secreting gland · disorder of saliva-secreting gland · non-neoplastic salivary gland disease · saliva-secreting gland disease · saliva-secreting gland disease or disorder · salivary gland disease · salivary gland disorder

Data availability: 3 GWAS associations (23 studies).

Disease family

This is a subtype of mouth disorder. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › mouth disordersalivary gland disorder

Related subtypes (26): uvulitis, adenoid hypertrophy, oral hairy leukoplakia, tongue disorder, alveolar periostitis, lip disorder, oral Crohn disease, maxillary sinusitis, oral candidiasis, oral tuberculosis, Ludwig’s angina, maxillary sinus cholesteatoma, burning mouth syndrome, oral leukoedema, tooth disorder, commissural lip fistula, oral submucous fibrosis, florid cemento-osseous dysplasia, oral cavity neoplasm, neoplasm of floor of mouth, polyp of maxillary sinus, neoplasm of jaw, osteoradionecrosis of the mandible, odontoma, lichen planus, oral, mouth mucosa disorder

Subtypes (9): submandibular gland disorder, benign lymphoepithelial lesion of salivary gland, mucocele of salivary gland, parotid disorder, necrotizing sialometaplasia, sialadenitis, sialolithiasis, Sjogren syndrome, tumor of salivary gland

Genetics & variants

GWAS landscape

3 GWAS associations across 23 studies. Top hits map to 3 distinct genes (as reported by GWAS).

Top associations by p-value

rsIDp-valueGeneRisk alleleOdds ratio
rs16479603e-10RN7SL167P - NTM?
rs611567104e-09SGCD?
rs1170327615e-08KBTBD11-OT1, ARHGEF10?

Top studies (by case count)

StudyLead authorYearCasesControlsTitle
GCST90478297Verma A20249,270428,988Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90478302Verma A20246,556434,802Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90473763UK Biobank Whole-Genome Sequencing Consortium20253,463454,977Whole-genome sequencing of 490,640 UK Biobank participants.
GCST90478296Verma A20242,550115,410Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480861Verma A20242,550115,410Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90478301Verma A20241,657117,317Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90480840Verma A20241,657117,317Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.
GCST90080177Backman JD20211,546384,408Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90084163Backman JD20211,546384,408Exome sequencing and analysis of 454,787 UK Biobank participants.
GCST90478295Verma A20241,38856,624Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program.

Variant details and genetic-evidence tiers

Tier distribution (top 50 variants)

TierVariants
Tier 1: coding0
Tier 2: splice/UTR0
Tier 3: regulatory0
Tier 4: intronic/intergenic3

MAF distribution

BucketVariants
common (>=0.05)1
low_freq (0.01-0.05)0
rare (<0.01)0
unknown2

Functional consequences

ConsequenceCount
intron_variant2
intergenic_variant1

Top variants

rsIDChrPosAllelesMAFConsequenceGenep-valueTier
rs164796011131051857G>A,T0.05intergenic_variantRN7SL167P - NTM3e-10Tier 4: intronic/intergenic
rs611567105156486436C>Tintron_variantSGCD4e-09Tier 4: intronic/intergenic
rs11703276181898412C>A,Gintron_variantKBTBD11-OT1, ARHGEF105e-08Tier 4: intronic/intergenic

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 14.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified10
PHASE22
PHASE31
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02068846PHASE3COMPLETEDBK Virus in Salivary Gland Disease: Treating the Potential Etiologic Agent
NCT00001598PHASE2COMPLETEDDHEA Treatment for Sjogren’s Syndrome
NCT01762514PHASE2UNKNOWNA Phase II Clinical Trial on Comparison of Effectiveness and Safeness of Different Amifostine Regimens
NCT03874572PHASE1UNKNOWNAllogeneic Mesenchymal Stem Cells for Radiation-induced Hyposalivation and Xerostomia/Dry Mouth
NCT02327884Not specifiedRECRUITINGCharacterization of Diseases With Salivary Gland Involvement
NCT00001390Not specifiedCOMPLETEDSalivary Evaluation in Healthy Volunteers
NCT00001852Not specifiedCOMPLETEDNatural History of Salivary Gland Dysfunction and Sjogren’s Syndrome
NCT01915966Not specifiedCOMPLETEDEfficacy Study of a Ginger and Cardamom Gelatin for Xerostomy in Terminally Ill Patients
NCT03746730Not specifiedUNKNOWNRole of US,Doppler in Major Salivary Gland Diseases
NCT03893812Not specifiedUNKNOWNColor Doppler and Mri Diffusion in Major Salivary Gland Masses
NCT04507646Not specifiedCOMPLETEDThe Effectiveness of Auricular Acupuncture on Improving Secretion of Saliva Among Institutional Older Population
NCT05151029Not specifiedUNKNOWNElastography in the Evaluation of Major Salivary Gland Lesions
NCT05346341Not specifiedCOMPLETEDEvaluation of the Effect of Minimally Invasive Procedures Used in Management of Salivary Ductal Pathologies on Patients’ Symptomatology and Gland Function
NCT06240806Not specifiedCOMPLETEDEfficacy of Manuka Honey Oral Rinse in Treatment of Xerostomia

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CIPROFLOXACIN41
PRASTERONE41
HONEY31
CHEMBL3139901